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Objectives
The purpose of a Quality Plan (QP).
When a Quality Plan (QP) is required and how to identify.
The requirements to the content and where to find them.
The responsibilities for review and handling.
The difference between a Quality Plan (QP) and an Inspection
and Test Plan (ITP).
The future of the Quality Plan (QP).
Purpose
For the supplier to show evidence on how their quality system
will apply in the execution of awarded purchase orders.
For the supplier to introduce applicable systems and
procedures.
For the supplier to present the list of subcontractors used for
FMC deliverables.
For FMC to have a list of contact persons at supplier.
When
The QP is required by the supplier when defined in a DRL
(Document Requirement List), linked in the Part Report (DBI).
Requirements
The requirements to the content in the QP are in the
FMC Standard Administration Requirements.
The QP shall as a minimum contain; specific quality practices,
resources and sequence of activities relevant to the product,
project or agreement.
Responsibilities
When required by DRL, supplier shall list the QP in the SMDR
as a review document for FMC and submit it latest 2WAO (weeks
after order).
If not previously submitted in the same revision. Always the latest revision.
Be aware
Quality Plan (QP) and Inspection & Test Plan (ITP) are two
different documents. QP is related to suppliers systems and
organization. ITP is for the manufacturing processes and
customer intervention (quality control).
An approved QP can be suggested for re-use in the SMDR
if the QP is made containing general information covering
suppliers complete relation with FMC.
FMC does not provide a template for QP. The content,
sequence and layout is up to the supplier to decide as
long as it meets the defined requirements. ISO-10005
is recommended as a guideline.
Next generation
The plan is to have the QP integrated as a part of
already existing documents.
Summary
What is the purpose of a Quality Plan (QP)?
When is a Quality Plan (QP) is required and how to identify?
Where to find the requirements to the content? Mention some.
Who owns the QP and who is responsible to submit it?
Who reviews the QP within FMC?
What are the main differences between a Quality Plan (QP)
and an Inspection & Test Plan (ITP)?